Medially Migrating Vestibular Schwannomas: A Review of 10 Cases.

IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY
Otology & Neurotology Pub Date : 2025-01-01 Epub Date: 2024-11-29 DOI:10.1097/MAO.0000000000004381
Brooklyn L Brovold, Christine M Lohse, Parv M Mehta, Girish Bathla, John I Lane, Joseph L Breen, Jamie J Van Gompel, Matthew L Carlson
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引用次数: 0

Abstract

Objective: To analyze cases of medial migration of vestibular schwannomas to propose an underlying mechanism.

Study design: Retrospective chart review.

Patients: Ten patients from one institution with sporadic vestibular schwannomas that demonstrated medial migration toward the cerebellopontine angle on serial imaging were reviewed.

Interventions: Among the 10 patients studied, 8 patients underwent stereotactic radiosurgery and 2 were managed with wait-and-scan. All serial imaging was analyzed throughout follow-up.

Main outcome measures: Volumetric and linear measurements were used to assess vestibular schwannoma growth. The fundal fluid cap length was measured from the most lateral end of the neoplasm within the internal auditory canal to the medial end of the cochlea. Pure tone averages of 0.5, 1, 2, and 3 kHz, word recognition scores, and AAO-HNS hearing class were used to assess levels of hearing loss per patient.

Results: Tumor growth exhibited a positive correlation with medial migration. Of the 10 patients studied, 9 exhibited tumor volume growth from initial to most recent imaging. Median changes in tumor volumes and fundal fluid cap lengths from initial diagnosis to the most recent imaging regardless of intervention were 130 mm 3 (range 1,400-2,970) and 2.8 mm (range 1.8-6.0), respectively. Migration was noted in 4 patients prior to any intervention, in 4 patients postradiosurgery, and in 2 patients before and after radiosurgery. Therefore, half of the tumors studied migrated before an intervention and half migrated postradiosurgery. No correlation of migration and hearing decline was observed.

Conclusion: Medial migration of vestibular schwannoma is associated with an increase in tumor volume, supporting a "tumor squeeze" mechanism within a conical internal auditory canal toward the wider porus acusticus and cerebellopontine angle.

前庭神经鞘瘤10例临床分析
目的:分析前庭神经鞘瘤内侧迁移的病例,探讨其发生机制。研究设计:回顾性图表回顾。患者:我们回顾了来自同一机构的10例散发性前庭神经鞘瘤患者,在连续影像学上表现为向小脑桥脑角内侧迁移。干预措施:在研究的10例患者中,8例患者接受了立体定向放射手术,2例患者接受了等待扫描。随访期间分析所有序列影像。主要结果测量:体积测量和线性测量用于评估前庭神经鞘瘤的生长。从内耳道内肿瘤最外侧端至耳蜗内侧端测量底液帽长度。使用0.5、1、2和3 kHz的纯音平均值、单词识别分数和AAO-HNS听力等级来评估每位患者的听力损失水平。结果:肿瘤生长与内侧迁移呈正相关。在研究的10例患者中,9例从最初到最近的影像学显示肿瘤体积增长。从最初诊断到最近的影像学检查,无论干预措施如何,肿瘤体积和基底液帽长度的中位变化分别为130 mm3(范围1400 - 2970)和2.8 mm(范围1.8-6.0)。4例患者在任何干预前,4例患者在手术后,2例患者在放疗前后出现迁移。因此,研究中一半的肿瘤在干预前迁移,一半在手术后迁移。没有观察到迁移与听力下降的相关性。结论:前庭神经鞘瘤的内向迁移与肿瘤体积增加有关,支持锥形内耳道内向更宽的耳孔和桥小脑角的“肿瘤挤压”机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Otology & Neurotology
Otology & Neurotology 医学-耳鼻喉科学
CiteScore
3.80
自引率
14.30%
发文量
509
审稿时长
3-6 weeks
期刊介绍: ​​​​​Otology & Neurotology publishes original articles relating to both clinical and basic science aspects of otology, neurotology, and cranial base surgery. As the foremost journal in its field, it has become the favored place for publishing the best of new science relating to the human ear and its diseases. The broadly international character of its contributing authors, editorial board, and readership provides the Journal its decidedly global perspective.
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